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Cell Death and Survival Pathways Involving ATM Protein Kinase

Cell death is the ultimate form of cellular dysfunction, and is induced by a wide range of stresses including genotoxic stresses. During genotoxic stress, two opposite cellular reactions, cellular protection through DNA repair and elimination of damaged cells by the induction of cell death, can occu...

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Detalles Bibliográficos
Autores principales: Aki, Toshihiko, Uemura, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535589/
https://www.ncbi.nlm.nih.gov/pubmed/34680975
http://dx.doi.org/10.3390/genes12101581
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author Aki, Toshihiko
Uemura, Koichi
author_facet Aki, Toshihiko
Uemura, Koichi
author_sort Aki, Toshihiko
collection PubMed
description Cell death is the ultimate form of cellular dysfunction, and is induced by a wide range of stresses including genotoxic stresses. During genotoxic stress, two opposite cellular reactions, cellular protection through DNA repair and elimination of damaged cells by the induction of cell death, can occur in both separate and simultaneous manners. ATM (ataxia telangiectasia mutated) kinase (hereafter referred to as ATM) is a protein kinase that plays central roles in the induction of cell death during genotoxic stresses. It has long been considered that ATM mediates DNA damage-induced cell death through inducing apoptosis. However, recent research progress in cell death modality is now revealing ATM-dependent cell death pathways that consist of not only apoptosis but also necroptosis, ferroptosis, and dysfunction of autophagy, a cellular survival mechanism. In this short review, we intend to provide a brief outline of cell death mechanisms in which ATM is involved, with emphasis on pathways other than apoptosis.
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spelling pubmed-85355892021-10-23 Cell Death and Survival Pathways Involving ATM Protein Kinase Aki, Toshihiko Uemura, Koichi Genes (Basel) Review Cell death is the ultimate form of cellular dysfunction, and is induced by a wide range of stresses including genotoxic stresses. During genotoxic stress, two opposite cellular reactions, cellular protection through DNA repair and elimination of damaged cells by the induction of cell death, can occur in both separate and simultaneous manners. ATM (ataxia telangiectasia mutated) kinase (hereafter referred to as ATM) is a protein kinase that plays central roles in the induction of cell death during genotoxic stresses. It has long been considered that ATM mediates DNA damage-induced cell death through inducing apoptosis. However, recent research progress in cell death modality is now revealing ATM-dependent cell death pathways that consist of not only apoptosis but also necroptosis, ferroptosis, and dysfunction of autophagy, a cellular survival mechanism. In this short review, we intend to provide a brief outline of cell death mechanisms in which ATM is involved, with emphasis on pathways other than apoptosis. MDPI 2021-10-07 /pmc/articles/PMC8535589/ /pubmed/34680975 http://dx.doi.org/10.3390/genes12101581 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Aki, Toshihiko
Uemura, Koichi
Cell Death and Survival Pathways Involving ATM Protein Kinase
title Cell Death and Survival Pathways Involving ATM Protein Kinase
title_full Cell Death and Survival Pathways Involving ATM Protein Kinase
title_fullStr Cell Death and Survival Pathways Involving ATM Protein Kinase
title_full_unstemmed Cell Death and Survival Pathways Involving ATM Protein Kinase
title_short Cell Death and Survival Pathways Involving ATM Protein Kinase
title_sort cell death and survival pathways involving atm protein kinase
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535589/
https://www.ncbi.nlm.nih.gov/pubmed/34680975
http://dx.doi.org/10.3390/genes12101581
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